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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 444063Generated: October 26, 2026

Water → 1,2-Di-O-(n-hexadecyl)-3-O-(3-cyanobenzyl)-glycerol

https://huagongshe.com/reaction/444063

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantSodium hydrideHCID 24758—
ReactantBenzonitrile, 3-(bromomethyl)-HCID 97249—
Reactant2,3-Bis(hexadecyloxy)propan-1-olHCID 102548—
SolventTetrahydrofuranHCID 8028—
Product1,2-Di-O-(n-hexadecyl)-3-O-(3-cyanobenzyl)-glycerolHCID 2346615868%

Reaction Steps

Sodium hydride (1.056 g. of 50 wt. % mineral oil dispersion, 22 mmoles) was added to a solution of 1,2-di-O-(n-hexadecyl)-glycerol (9.73 g., 18 mmoles) in tetrahydrofuran (150 ml.) and the resulting solution stirred for 20 minutes at room temperature under nitrogen. m-Cyanobenzyl bromide (4.0 g., 20 mmoles) was added and the reaction mixture stirred overnight at room temperature under nitrogen. Water (200 ml.) was then added cautiously and the resulting mixture extracted with ethyl acetate (3×150 ml.). The combined ethyl acetate extract was dried (MgSO4), filtered and evaporated in vacuo to an oil (12 g.), which was purified by silica gel chromatography (elution with benzene:hexane) [8.0 g., 68% yield, oil, ir (CHCl3) 2230 cm-1 ].

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04262021
Source datasetuspto-grants-1981_04
ORD IDord-d0d52e488d75449eaa6c34ec73bff122
Source noteuspto-grants-1981_04